Canonical Allele Identifier: PA915998882
Gene: NTHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 646936
ClinVar Variation Id: 1521137
ClinVar RCV Id: RCV002046245

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002519.2:p.Met94Ile
CA394295707
NM_002528.7:c.282G>T
CA394295709
NM_002528.7:c.282G>C
CA394295714
NM_002528.7:c.282G>A